SMILES CC(Nc1nc(-c2c(C)onc2-c2ccccc2)ccn1)=O
Download 50441089.mol2, BDB-kin50441089.pdbqt
Total Surface Area 232,48
TPSA 80,91
cLogS -4,246
MW 294,313
cLogP 2,4782
H-Acceptors 6
H-Donors 1
Ro5 violations 0
Druglikeness 0,78734
DrugScore 0,655677575234734
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Human Intestinal Absorption HIA+
Blood-Brain Barrier BBB+
Caco-2 Permeability I Caco2+
Caco-2 Permeability II 2,0508
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor I Inhibitor
P-glycoprotein Inhibitor II Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity High CYP Inhibitory Promiscuity
AMES Toxicity AMES toxic
Carcinogenicity (Three-class) Danger
Biodegradation Not ready biodegradable
Rat Acute Toxicity 2,4695
hERG inhibition (predictor I) Weak inhibitor
hERG inhibition (predictor II) Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) 0,5193
Fish Toxicity Low FHMT
Fish Toxicity (pLC50 mg/L) 1,6949
Acute Oral Toxicity III
Carcinogens Non-carcinogens
Honey Bee Toxicity Low HBT
Subcellular localization Mitochondria
These data are only available for scientific research purposes.